Product Details

SNP ID
rs355625
Assay Type
Functionally tested
NCBI dbSNP Submissions
32
Location
Chr.1:180230410 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCCTGAGAAGCGGAGGGCCCGGCTT[C/T]CACCGTGACTCCAGCGGCCTGCTTG
Phenotype
MIM: 602146
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LHX4 PubMed Links

Gene Details

Gene
LHX4
Gene Name
LIM homeobox 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_033343.3 113 UTR 5 NP_203129.1
XM_011510105.2 113 Intron XP_011508407.1
XM_011510106.2 113 Intron XP_011508408.1
XM_011510108.2 113 Intron XP_011508410.1
XM_017002755.1 113 Intron XP_016858244.1

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